Post on 25-Apr-2022
PETER MACCALLUM CANCER CENTRE MOLECULAR HAEMATOLOGY REQUEST FORM
MP-MH-HMD-02B v05
PATIENT DETAILS REQUESTING CLINICIAN DETAILS SURNAME:
FIRST NAME:
DOB: MALE FEMALE
ADDRESS:
MEDICARE NO:
NAME:
HOSPITAL / LAB:
PROVIDER NO:
EMAIL:
SIGNATURE: DATE:
CLINICAL & SAMPLE DETAILS CLINICAL NOTES / REASON FOR TEST REQUEST (REQUIRED):
PLEASE SEND ALL RELEVANT PATHOLOGY RESULTS (E.G. BONE MARROW REPORT, FBE REPORT, HISTOPATHOLOGY REPORT, ETC.) WITH SAMPLE
SAMPLE TYPE BONE MARROW BLOOD TISSUE cfDNA OTHER (PLEASE STATE): COLLECTION DATE (IF ADD-ON REQUEST):
TO BE COMPLETED BY COLLECTOR (IF PRIMARY FORM) COLLECTED AND LABELLED BY: SURNAME COLLECTION DATE TIME SIGNATURE
I CERTIFY THAT THE PATHOLOGY SPECIMEN AND REQUEST FORM COMPLY WITH MINIMUM LABELLING REQUIREMENTS AND THAT THE SPECIMEN WAS TAKEN FROM THE PATIENT STATED ABOVE AS ESTABLISHED BY DIRECT ENQUIRY AND/OR INSPECTION OF THE IDENTIFICATION BAND AND WAS LABELLED IMMEDIATELY.
AVAILABLE ASSAYS
GENOMIC TESTING SUPPORTED BY SNOWDOME FOUNDATION THROUGH THE WILSON CENTRE FOR LYMPHOMA GENOMICS
NGS GENE PANELS MUTATION SPECIFIC ASSAYS GENE LISTS AND FURTHER INFORMATION ON REVERSE
MYELOPROLIFERATIVE NEOPLASM (MPN) DIAGNOSTICGENE PANEL (8 GENES)
HAEMATOLOGICAL MALIGNANCY (ALLHAEM) GENEPANEL (57 GENES) SELECT THIS BOX TO EXCLUDE DDX41 ANALYSIS
PANEL AVAILABLE ON BLOOD, BM, TISSUE AND cfDNA
SINGLE GENE TP53 ANALYSIS
TESTING TO DETERMINE ORIGIN (SOMATIC VSGERMLINE) OF PREVIOUSLY DETECTED VARIANT
PLEASE REFER TO SEPARATE FORM FOR INHERITED BONE MARROW DISORDER NGS PANEL REQUESTS (AVAILABLE ONLINE)
PLEASE NOTE: THESE ASSAYS MAY DETECT GERMLINE VARIANTS WITH SIGNIFICANT IMPLICATIONS FOR BOTH THE PATIENT AND THEIR FAMILY. PLEASE ENSURE THAT YOU AND YOUR PATIENT UNDERSTAND THIS POSSIBILITY.
FLT3-ITD & TKD
NPM1 (NON-QUANTITATIVE)
JAK2 Val617Phe
MYD88 Leu265Pro
BRAF Val600Glu
QUANTITATIVE PCR (qPCR) ASSAYS t(9;22) BCR-ABL1
t(15;17) PML-RARA
t(8;21) RUNX1-RUNX1T1
inv(16) / t(16;16) CBFB-MYH11
NPM1 MRD (TYPE A – qPCR; non-TYPE A – NGS)
OTHER ASSAYS
CHIMERISM
IGHV SOMATIC HYPERMUTATION (SHM) ANALYSIS
HAVCR2 GENE VARIANT ANALYSIS
UBA1 GENE MUTATION ANALYSIS
PAYMENT
BILL HOSPITAL / PATHOLOGY PROVIDER BILL MEDICARE (MUST SIGN BELOW. NON-REBATABLE COMPONENTS WILL BE BILLED TO PATHOLOGY PROVIDED UNLESS OTHERWISE SPECIFIED)
MEDICARE ASSIGNMENT FORM (SECTION 20A OF THE HIA 1973) I OFFER TO ASSIGN MY RIGHT TO BENEFITS TO THE APPROVED PRACTITIONER WHO WILL RENDER THEREQUESTED PATHOLOGY SERVICE(S) AND ANY ELIGIBLE PATHOLOGICAL DETERMINABLE SERVICE(S) ESTABLISHED NECESSARY BY THE PRACTITIONER.
PATIENT SIGNATURE: DATE:OR IF PATIENT UNABLE TO SIGN: I AUTHORISE PETER MACCALLUM CANCER CENTRE, WHO WILL RENDER THE REQUESTED PATHOLOGY SERVICES, AND ANY FURTHER PATHOLOGYSERVICES WHICH THE PRACTITIONER DETERMINES TO BE NECESSARY, TO SUBMIT MY UNPAID ACCOUNT TO MEDICARE, SO THAT MEDICARE CAN ASSESS MY CLAIM AND ISSUE ME ACHEQUE MADE PAYABLE TO THE PRACTITIONER, FOR THE MEDICARE BENEFIT. VERBAL CONSENT WAS PROVIDED BY PATIENT TO SUBMIT UNPAID ACCOUNT TO MEDICARE
(NO SIGNATURE AVAILABLE) BILL PATIENT DIRECTLY (MUST SIGN HERE TO ACKNOWLEDGE COSTS HAVE BEEN DISCUSSED): PATIENT SIGNATURE: BILL OTHER (PLEASE SPECIFY):
PETER MACCALLUM CANCER CENTRE MOLECULAR HAEMATOLOGY REQUEST FORM
MP-MH-HMD-02B v05
NGS GENE PANEL LISTS HAEMATOLOGICAL MALIGNANCY GENE PANEL (ALLHAEM) – 57 GENES
ABL1 ARAF ASXL1 BCL2 BIRC3 BRAF BTK CALR CARD11 CBL CD274 CD79B CEBPA CSF3R CXCR4 DDX41* DNMT3A ETNK1 EZH2 FLT3** FYN GATA1 GATA2 ID3
IDH1 IDH2 IRF8 JAK2 JAK3 KIT KRAS MAP2K1 MPL MYD88 NOTCH1 NPM1 NRAS PDCD1LG2 PIGA PFH6
PLCG1 PLCG2 RHOA RUNX1 SETBP1 SF3B1 SH2B3 SRSF2 STAT3 STAT5B STAT6 TCF3 TET2 TP53 U2AF1 XPO1 ZRSR2
*DDX41 VARIANT ANALYSIS IS EXCLUDED ON REQUEST. CLINICALLY SIGNIFICANT VARIANTS IN THIS GENE ARE LIKELY TO BE OF GERMLINEORIGIN.
**FLT3-ITD ANALYSIS PERFORMED USING A SEPARATE ASSAY AND INCLUDED WHEN CLINICALLY APPROPRIATE OR REQUESTED.
THE HAEMATOLOGICAL MALIGNANCY GENE PANEL HAS BEEN DESIGNED TO PROVIDE DIAGNOSTIC, PROGNOSTIC AND THERAPEUTICINFORMATION ACROSS THE SPECTRUM OF HAEMATOLOGICAL MALIGNANCY AND IS AVAILABLE FOR ORDER ON THE FOLLOWING SAMPLETYPES: PERIPHERAL BLOOD, BONE MARROW ASPIRATE, FRESH OR FFPE TISSUE AND cfDNA. SEE SAMPLE REQUIREMENTS BELOW.
MYELOPROLIFERATIVE NEOPLASM (MPN) DIAGNOSTIC GENE PANEL – 8 GENES
JAK2 CALR MPL SF3B1 KIT CSF3R ETNK1 SH2B3 HHH
SAMPLE REQUIREMENTS
GENE SPECIFIC ASSAYS, NGS ASSAYS & IGHV SHM ASSAY
o 4ml PERIPHERAL BLOOD (EDTA)o 1-2ml BONE MARROW ASPIRATE (EDTA)o TISSUE: FRESH / FROZEN / FFPE BLOCK / FFPE SLIDES – PLEASE PROVIDE HISTOPATHOLOGY REPORTo DNA (MINIMUM 10µL at >50ng/µL)o CELL FREE DNA (cfDNA) (EXCLUDING IGHV ANALYSIS): 10ml PERIPHERAL BLOOD IN STRECK TUBE
SAMPLES FOR cfDNA MUST BE RECEIVED WITHIN 72 HOURS OF COLLECTIONo OTHER (E.G. CSF) – PLEASE CALL / EMAIL TO DISCUSS PRIOR TO SENDINGo HAIR (FOR FOLLOW UP TESTING OF PREVIOUSLY DETECTED VARIANTS ONLY) – PLEASE CALL / EMAIL
TO DISCUSS PRIOR TO SENDING
QPCR ASSAYS
o 20ml PERIPHERAL BLOOD (EDTA)o 1-2ml BONE MARROW ASPIRATE (EDTA)
ALL SAMPLES MUST BE RECEIVED WITHIN 48 HOURS OF COLLECTION
CHIMERISM o 4ml (PRE-TRANSPLANT) / 18ml (POST-TRANSPLANT) PERIPHERAL BLOOD (EDTA)o 1-2ml BONE MARROW ASPIRATE (EDTA)
POST-TRANSPLANT SAMPLES MUST BE RECEIVED WITHIN 24 HOURS OF COLLECTION
ADDRESS & CONTACT DETAILS PLEASE SEND SPECIMEN AND COMPLETED FORM TO:
PATHOLOGY – SPECIMEN RECEPTION (LEVEL 4) PETER MACCALLUM CANCER CENTRE
305 GRATTAN STREET MELBOURNE VIC 3000
TEL: +61 3 8559 7284 EMAIL: MOLECULAR.HAEMATOLOGY@PETERMAC.ORG
FAX: +61 3 8559 5437 WEBSITE: www.petermac.org/about/signature-centres/centre-clinical-cancer-genomics/molecular-haematology